Ober B T, Summerfield A, Mattlinger C, Wiesmüller K H, Jung G, Pfaff E, Saalmüller A, Rziha H J
Federal Research Centre for Virus Diseases of Animals, D-72076 Tübingen, Germany.
J Virol. 1998 Jun;72(6):4866-73. doi: 10.1128/JVI.72.6.4866-4873.1998.
Pseudorabies virus (PRV; suid herpesvirus 1) infection causes heavy economic losses in the pig industry. Therefore, vaccination with live attenuated viruses is practiced in many countries. This vaccination was demonstrated to induce extrathymic virus-specific memory CD4+CD8+ T lymphocytes. Due to their major histocompatibility complex (MHC) class II-restricted proliferation, it is generally believed that these T lymphocytes function as memory T-helper cells. To directly prove this hypothesis, 15-amino-acid, overlapping peptides of the viral glycoprotein gC were used for screening in proliferation assays with peripheral blood mononuclear cells of vaccinated d/d haplotype inbred pigs. In these experiments, two naturally processed T-cell epitopes (T1 and T2) which are MHC class II restricted were identified. It was shown that extrathymic CD4+CD8+ T cells are the T-lymphocyte subpopulation that responds to epitope T2. In addition, we were able to show that cytokine secretion can be induced in these T cells through recall with inactivated PRV and demonstrated that activated PRV-primed CD4+CD8+ T cells are able to induce PRV-specific immunoglobulin synthesis by PRV-primed, resting B cells. Taken together, these results demonstrate that the glycoprotein gC takes part in the priming of humoral anti-PRV memory responses. The experiments identified the first T-cell epitopes so far known to induce the generation of virus-specific CD4+CD8+ memory T lymphocytes and showed that CD4+CD8+ T cells are memory T-helper cells. Therefore, this study describes the generation of virus-specific CD4+CD8+ T cells, which is observed during vaccination, as a part of the potent humoral anti-PRV memory response induced by the vaccine.
伪狂犬病病毒(PRV;猪疱疹病毒1型)感染给养猪业造成了巨大的经济损失。因此,许多国家都采用减毒活病毒进行疫苗接种。已证明这种疫苗接种可诱导胸腺外病毒特异性记忆CD4⁺CD8⁺ T淋巴细胞。由于它们受主要组织相容性复合体(MHC)II类限制的增殖,人们普遍认为这些T淋巴细胞发挥记忆性辅助性T细胞的功能。为了直接验证这一假设,使用病毒糖蛋白gC的15个氨基酸的重叠肽,对接种疫苗的d/d单倍型近交猪的外周血单个核细胞进行增殖试验筛选。在这些实验中,鉴定出了两个受MHC II类限制的天然加工的T细胞表位(T1和T2)。结果表明,胸腺外CD4⁺CD8⁺ T细胞是对表位T2作出反应的T淋巴细胞亚群。此外,我们能够证明,通过用灭活的PRV进行回忆反应,可在这些T细胞中诱导细胞因子分泌,并证明活化的经PRV致敏的CD4⁺CD8⁺ T细胞能够诱导经PRV致敏的静止B细胞合成PRV特异性免疫球蛋白。综上所述,这些结果表明糖蛋白gC参与了体液抗PRV记忆反应的启动。这些实验鉴定出了迄今为止已知的首个可诱导病毒特异性CD4⁺CD8⁺记忆T淋巴细胞产生的T细胞表位,并表明CD4⁺CD8⁺ T细胞是记忆性辅助性T细胞。因此,本研究将疫苗接种过程中观察到的病毒特异性CD4⁺CD8⁺ T细胞的产生描述为疫苗诱导的有效体液抗PRV记忆反应的一部分。